ORPHA:169154
T-B+NK+ severe combined immunodeficiency due to IL-7Ralpha deficiency
Also called T-B+NK+ SCID due to IL-7Ralpha deficiency
- Body system
- Immunological diseases
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy
- Estimated prevalence
- 1-9 / 1 000 000 (Worldwide)
- Rarity class
- 1-9 / 1 000 000
ORPHA:169154 is classified under "Immunological diseases" in the Orphanet nomenclature.
Common signs
- Recurrent infections
- Failure to thrive
- Lymphopenia
- Recurrent viral infections
- Decreased total T cell count
- Decreased proportion of CD8-positive T cells